Identity
- Trade Name
- Performance-LOAD FDA UDI
- Generic Name
- Ambulance stretcher docking device FDA UDI
- Model / Reference
- 6392 FDA UDI
Identifiers
- Catalog Number
- 6392-000-001 FDA UDI
- Primary DI / UDI-DI
- 07613327282542 FDA UDI
- FDA Product Code
- FPO FDA UDI
- GMDN Term
- Ambulance stretcher docking device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6910 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ambulance stretcher docking device
Performance-LOAD by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ambulance stretcher docking device.
- Patient Loading Utility System (PLUS) — LIFEPORT, LLC. · Class I
- Patient Loading Utility System (PLUS) — LIFEPORT, LLC. · Class I
- Utility Pedestal Assembly — LIFEPORT, LLC. · Class I
- PLUS — LIFEPORT, LLC. · Class I
- Load Ramp — LIFEPORT, LLC. · Class I
- PLUS — LIFEPORT, LLC. · Class I
- PLUS — LIFEPORT, LLC. · Class I
- Patient Loading Utility System (PLUS) — LIFEPORT, LLC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 0a3bb3be-5e52-4826-b8c2-ecfd1a4572a0 34 fields · synced May 30, 2026